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Updated: Jun 23, 2026

Injectable Supramolecular Polymer-Nanoparticle Hydrogels for Cell and Drug Delivery Applications
Published on: February 7, 2021
Time-dependent alginate/polyvinyl alcohol hydrogels as injectable cell carriers
Sang Ho Cho1, Sung Mook Lim, Dong Keun Han
1Department of Advanced Materials, Hannam University, 461-6 Jeonmin Dong, Yuseong Gu, Daejeon 305-811, South Korea.
Injectable alginate/polyvinyl alcohol (PVA) blend hydrogels were developed with controlled gelation rates using calcium sulfate and sodium phosphate. These biocompatible hydrogels support chondrocyte growth and activity, showing promise as injectable cell carriers.
Area of Science:
- Biomaterials Science
- Tissue Engineering
- Polymer Chemistry
Background:
- Alginate hydrogels are widely used as cell carriers but suffer from rapid gelation and lack of injectability.
- Existing injectable alginate systems using calcium sulfate or carbonate have limitations in gelation control.
- There is a need for injectable hydrogels with tunable properties for effective cell delivery.
Purpose of the Study:
- To develop injectable alginate/polyvinyl alcohol (PVA) blend hydrogels with a controllable gelation rate.
- To investigate the effect of cross-linking agent and retardation agent ratios on gelation kinetics.
- To evaluate the in vitro cell compatibility and chondrogenic potential of the developed hydrogels.
Main Methods:
- Alginate/PVA blend hydrogels were prepared using calcium sulfate (CaSO4) as a cross-linking agent and sodium phosphate (Na2HPO4) as a retardation agent.
- The ratio of CaSO4/Na2HPO4 was adjusted to control the gelation rate.
- In vitro cell culture of human chondrocytes was performed to assess cell viability, proliferation, and glycosaminoglycan (GAG) production over 28 days.
Main Results:
- Controllable gelation rates were achieved by adjusting the CaSO4/Na2HPO4 ratio, with increased Na2HPO4 and decreased CaSO4 leading to slower gelation.
- Alginate and PVA exhibited good compatibility, with minimal PVA extraction observed over 7 days.
- Chondrocytes showed linear growth and increased GAG content in alginate/PVA hydrogels, particularly those with higher PVA content, indicating enhanced cell viability and activity.
Conclusions:
- Injectable alginate/PVA blend hydrogels with tunable gelation kinetics were successfully fabricated.
- The developed hydrogels demonstrate excellent biocompatibility and support chondrocyte proliferation and function.
- These findings suggest that alginate/PVA hydrogels are promising candidates for injectable cell carrier applications in tissue engineering.
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